Evidence map›Paper›PMID 33227998›Full record

ArticleInternational journal of molecular sciences2020

Role of iRhoms 1 and 2 in Endochondral Ossification.

Renpeng Fang, Coline Haxaire, Miguel Otero, Samantha Lessard, Gisela Weskamp, David R McIlwain, Tak W Mak, Stefan F Lichtenthaler, Carl P Blobel

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 35% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 4 countries.

Renpeng FangDepartment of Orthopaedics, Xiangya Hospital, Central South University, Changsha 410008, China.
Coline HaxaireArthritis and Tissue Degeneration Program, Hospital for Special Surgery at Weill Cornell Medicine, New York, NY 10021, USA.
Miguel OteroOrthopedic Soft Tissue Research Program, Hospital for Special Surgery at Weill Cornell Medicine, New York, NY 10021, USA.
Samantha LessardOrthopedic Soft Tissue Research Program, Hospital for Special Surgery at Weill Cornell Medicine, New York, NY 10021, USA.
Gisela WeskampArthritis and Tissue Degeneration Program, Hospital for Special Surgery at Weill Cornell Medicine, New York, NY 10021, USA.
David R McIlwainBaxter Laboratory in Stem Cell Biology, Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Tak W MakCampbell Family Institute for Breast Cancer Research, Ontario Cancer Institute, University Health Network, Toronto, ON M5G 2M9, Canada.
Stefan F LichtenthalerGerman Center for Neurodegenerative Diseases (DZNE), 81377 Munich, Germany.
Carl P BlobelArthritis and Tissue Degeneration Program, Hospital for Special Surgery at Weill Cornell Medicine, New York, NY 10021, USA.ORCID 0000-0001-5053-3137
Hospital for Special Surgery · USGerman Center for Neurodegenerative Diseases · DEOntario Institute for Cancer Research · CAStanford University · US

Funding

Role of iRhoms and ADAM17 in EGFR and TNFalpha signalingR35GM134907 · NIGMS · HOSPITAL FOR SPECIAL SURGERY · PI BLOBEL, CARL PETER · 2020 to 2024
$2.0M
Deutsche Forschungsgemeinschaft EXC 2145 SyNergy- ID 390857198NIGMS NIH HHS R35 GM134907NIH HHS R01 GM64750; R35 GM134907
6 · The paper itself

Abstract

Growth of the axial and appendicular skeleton depends on endochondral ossification, which is controlled by tightly regulated cell-cell interactions in the developing growth plates. Previous studies have uncovered an important role of a disintegrin and metalloprotease 17 (ADAM17) in the normal development of the mineralized zone of hypertrophic chondrocytes during endochondral ossification. ADAM17 regulates EGF-receptor signaling by cleaving EGFR-ligands such as TGFα from their membrane-anchored precursor. The activity of ADAM17 is controlled by two regulatory binding partners, the inactive Rhomboids 1 and 2 (iRhom1, 2), raising questions about their role in endochondral ossification. To address this question, we generated mice lacking iRhom2 (

Indexed as

ADAM17 ProteinAnimalsCalcification, PhysiologicCarrier ProteinsCell CommunicationCell DifferentiationCell ProliferationChondrocytesChondrogenesisCollagen Type IIErbB ReceptorsGene Expression RegulationGrowth PlateIntegrasesMembrane ProteinsMiceADAM17 ProteinAdam17 protein, mouseCarrier ProteinsCol2a1 protein, mouseCollagen Type IICre recombinaseEGFR protein, mouseErbB ReceptorsIntegrasesiRhom1 protein, mouseiRhom2 protein, mouseMembrane ProteinsTransforming Growth Factor alphaADAM17a disintegrin and metalloprotease 17endochondral ossificationinactive Rhomboid 1, 2iRhom1, 2

Identifiers

PMID33227998
PMCPMC7699240
OpenAlexW3101556373

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.